Adriana Cunha

Senior Manager, Clinical Site Management @Abdera Therapeutics

Miami, FL, US
EMAILS
a•••••@abderatx.com
MOBILE NUMBERS
+19•••••••64

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WORK HISTORY

Oct 2025 — Present

Senior Manager, Clinical Site Management @Abdera Therapeutics

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Sponsor Leadership | Site Strategy & Trial Delivery | Accelerating FIH ExecutionStrategic oversight of Phase I radiopharmaceutical oncology programs, driving operational excellence, site performance, and compliance across all stages of study execution. Partnering with Clinical Development, Regulatory, and Quality leadership to ensure inspection readiness, optimize startup efficiency, and uphold the highest standards of patient safety and data integrity.

EDUCATION

N/A

MIT Sloan School of Management

Executive Education, AI in Pharma and Biotech

2002 — 2007

USP - Universidade de São Paulo

Pharmacy & Biochemistry, BPharm

SKILLS

Pharmaceutical IndustrySopFdaDrug SafetyCardiologyInformIch-GcpPatient RecruitmentOncology Clinical ResearchClinical Data ManagementClinical MonitoringRegulatory SubmissionsOracle ClinicalClinical TrialsRheumatologyClinical Study DesignBiotechnologyRheumatoid ArthritisIrbCRORegulatory RequirementsEcrfClinical DevelopmentClinical Research ExperienceOncologyProtocolEndocrinologyRegulatory AffairsCardiovascular DiseaseVaccinesEdcTherapeutic AreasCtmsTrial ManagementClinical Operations21 Cfr Part 11Clinical Site MonitoringDrug DevelopmentClinical ResearchGcp

ABOUT ADRIANA CUNHA

Clinical Research Leader with over 20 years of experience overseeing global Phase clinical trials across oncology, neurology, cardiology, rare, and infectious diseases. Recognized for strategic oversight of early-phase oncology programs, operational excellence, and deep expertise in CRO/vendor management, site engagement, and regulatory compliance (FDA, EMA, ANVISA).Currently supporting radiopharmaceutical portfolio development at Abdera Therapeutics, with emphasis on quality-driven execution, inspection readiness, and strong cross-functional collaboration with Clinical Development, Regulatory, and Quality teams.Known for building high-performing site partnerships and fostering alignment across stakeholders, with a consistent record of delivering trials on time, within scope, and to the highest standards of GCP and data integrity. Passionate about advancing innovative therapies that improve patient outcomes and shape the future of clinical research.

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